CA2225807A1 - Use of lamellarin-class alkaloids in methods of treatment - Google Patents

Use of lamellarin-class alkaloids in methods of treatment

Info

Publication number
CA2225807A1
CA2225807A1 CA002225807A CA2225807A CA2225807A1 CA 2225807 A1 CA2225807 A1 CA 2225807A1 CA 002225807 A CA002225807 A CA 002225807A CA 2225807 A CA2225807 A CA 2225807A CA 2225807 A1 CA2225807 A1 CA 2225807A1
Authority
CA
Canada
Prior art keywords
mdr
lamellarin
found
treatment
cells
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CA002225807A
Other languages
French (fr)
Other versions
CA2225807C (en
Inventor
Jose Luis Fernandez Puentes
Delores Garcia Gravalos
Ana Rodriguez Quesada
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Pharmamar SA
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Publication of CA2225807A1 publication Critical patent/CA2225807A1/en
Application granted granted Critical
Publication of CA2225807C publication Critical patent/CA2225807C/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/475Quinolines; Isoquinolines having an indole ring, e.g. yohimbine, reserpine, strychnine, vinblastine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/4738Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/4745Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/70Carbohydrates; Sugars; Derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • Molecular Biology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)
  • Steroid Compounds (AREA)
  • Coating Apparatus (AREA)

Abstract

The lamellarin compounds disclosed herein have been found to be inhibitors of MDR, i.e., acquired multidrug resistance, which has become a major problem in the treatment of various cancers. The lamellarin compounds disclosed herein have also been found to be cytotoxic to MDR cells. MDR is believed to be associated with certain alterations in tumor cells, including an over-expression of a certain high molecular weight membrane glycoprotein and a decrease in the ability of the tumor cell to accumulate and retain chemotherapeutic agents. The present invention is thus directed to methods of treating MDR-type tumors with an effective anti-MDR amount (either inhibitory or cytotoxic) of one or more lamellarin compounds, which compounds have been found to be effective antitumoral agents against MDR
cells.
CA002225807A 1995-06-29 1996-06-26 Use of lamellarin-class alkaloids in methods of treatment Expired - Fee Related CA2225807C (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US08/496,465 US5852033A (en) 1995-06-29 1995-06-29 Methods of treatment using lamellarin-class alkaloids
US08/496,465 1995-06-29
PCT/IB1996/000742 WO1997001336A1 (en) 1995-06-29 1996-06-26 Use of lamellarin-class alkaloids in methods of treatment

Publications (2)

Publication Number Publication Date
CA2225807A1 true CA2225807A1 (en) 1997-01-16
CA2225807C CA2225807C (en) 2008-04-22

Family

ID=23972747

Family Applications (1)

Application Number Title Priority Date Filing Date
CA002225807A Expired - Fee Related CA2225807C (en) 1995-06-29 1996-06-26 Use of lamellarin-class alkaloids in methods of treatment

Country Status (15)

Country Link
US (2) US5852033A (en)
EP (1) EP0835108B1 (en)
JP (1) JP4153992B2 (en)
AT (1) ATE208196T1 (en)
AU (1) AU700420B2 (en)
CA (1) CA2225807C (en)
DE (1) DE69616792T2 (en)
DK (1) DK0835108T3 (en)
ES (1) ES2164899T3 (en)
HU (1) HU225588B1 (en)
MX (1) MX9800248A (en)
PL (1) PL184667B1 (en)
PT (1) PT835108E (en)
RU (1) RU2188637C2 (en)
WO (1) WO1997001336A1 (en)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5852033A (en) * 1995-06-29 1998-12-22 Pharma Mar, S.A. Methods of treatment using lamellarin-class alkaloids
AUPO656597A0 (en) * 1997-05-02 1997-05-29 Australian National University, The Preparation of therapeutic compounds
US6248752B1 (en) * 1998-02-27 2001-06-19 Charles Duane Smith Azabicyclooctane compositions and methods for enhancing chemotherapy
AUPP433398A0 (en) * 1998-06-25 1998-07-16 Australian National University, The Compounds and processes
GB9920912D0 (en) * 1999-09-03 1999-11-10 Indena Spa Novel derivatives of flavones,xanthones and coumarins
US7250409B2 (en) * 2000-03-01 2007-07-31 The Scripps Research Institute Ningalin B analogs employable for reversing multidrug resistance
US6989396B2 (en) 2001-04-12 2006-01-24 The Board Of Trustees Of The University Of Illinois Tropane alkaloid multidrug resistance inhibitors from Erythroxylum pervillei and use of the same
US20030109448A1 (en) * 2001-11-07 2003-06-12 Crowley Kathleen S. Methods of promoting uptake and nuclear accumulation of polyamides in eukaryotic cells
PT1505964E (en) * 2002-05-17 2008-02-28 Merckle Gmbh Annelated pyrrole compounds as proton pump inhibitors for treating ulcer
US20060040945A1 (en) * 2002-05-17 2006-02-23 Merckle Gmbh Annellated pyrrole compounds as proton pump inhibitors for treating ulcer
GB0218816D0 (en) * 2002-08-13 2002-09-18 Pharma Mar Sa Antitumoral analogs of lamellarins
US8138170B2 (en) * 2004-08-27 2012-03-20 Memorial Sloan-Kettering Cancer Center Immunosuppressive Ningalin compounds
JP5888702B2 (en) * 2011-01-17 2016-03-22 国立大学法人 長崎大学 Anticancer active compound
WO2018181777A1 (en) * 2017-03-29 2018-10-04 国立大学法人 長崎大学 Fourth-generation egfr tyrosine kinase inhibitor
JOP20190254A1 (en) 2017-04-27 2019-10-27 Pharma Mar Sa Antitumoral compounds
RU2745401C1 (en) * 2020-07-13 2021-03-24 Федеральное государственное бюджетное учреждение науки Федеральный исследовательский центр "Институт биологии южных морей имени А.О. Ковалевского РАН" (ФИЦ ИнБЮМ) Method for inducing the secretion of biologically active compounds in sea snail rapana venosa val.
CN112300232B (en) * 2020-11-03 2021-11-09 浙江大学 Lamelarin D glycosylated derivative and preparation and application thereof

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5852033A (en) * 1995-06-29 1998-12-22 Pharma Mar, S.A. Methods of treatment using lamellarin-class alkaloids

Also Published As

Publication number Publication date
AU6316796A (en) 1997-01-30
CA2225807C (en) 2008-04-22
WO1997001336A1 (en) 1997-01-16
DE69616792T2 (en) 2002-06-20
HUP9900186A3 (en) 2001-08-28
PL324282A1 (en) 1998-05-11
RU2188637C2 (en) 2002-09-10
AU700420B2 (en) 1999-01-07
MX9800248A (en) 1998-11-30
DK0835108T3 (en) 2002-03-18
ES2164899T3 (en) 2002-03-01
EP0835108A1 (en) 1998-04-15
HUP9900186A2 (en) 1999-06-28
EP0835108B1 (en) 2001-11-07
PL184667B1 (en) 2002-11-29
JPH11508882A (en) 1999-08-03
US5852033A (en) 1998-12-22
US6087370A (en) 2000-07-11
ATE208196T1 (en) 2001-11-15
HU225588B1 (en) 2007-03-28
DE69616792D1 (en) 2001-12-13
PT835108E (en) 2002-03-28
JP4153992B2 (en) 2008-09-24

Similar Documents

Publication Publication Date Title
CA2225807A1 (en) Use of lamellarin-class alkaloids in methods of treatment
WO1999057117A3 (en) Indole derivatives and their use in the treatment of malignant and other diseases caused by pathological cell proliferation
AU1833397A (en) Use of a texaphyrin in the preparation of a medicament for use with a chemotherapeutic agent in cancer chemosensitization
BG102999A (en) New 2,3-diasubstituted-4-(3h)-quinazolinons
GEP20053688B (en) Substituted-Triazolopyrimidines as Anticancer Agents
CA2086434A1 (en) Quinuclidine derivatives
AU7650294A (en) Aminocyclohexylesters and uses thereof
BG104813A (en) Substituted indolinones having an inhibiting effect on kinases and cycline/cdk complexes
NO974694L (en) Pharmaceutical preparation containing N-phosphonoglycine derivatives to inhibit cancer and virus growth
WO1997005870A3 (en) Use of griseofulvin for inhibiting the growth of cancers
CA2245766A1 (en) Compositions useful in the phototherapeutic treatment of proliferative skin disorders
EP1140022B8 (en) Method of administering a compound to multi-drug resistant cells
CA2281570A1 (en) Composition for treating tumors containing shark cartilage extracts and anti-neoplastic agents
CA2019812A1 (en) Novel 5,11-dihydro-6h-dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-ones and their use in the prevention or treatment of aids
CA2108963A1 (en) Compositions and Methods for Therapy and Prevention of Cancer, Aids and Anemia
MY103872A (en) 3-substituted-2-oxindole-1-carboxamides for suppressing t-cell function.
WO1990009806A3 (en) Composition for the inhibition of tumors and for the non-cytotoxic inhibition of replication of viruses
MY110149A (en) Compounds for the treatment of neurodegenerative disorders
WO1993000427A3 (en) Neurite growth regulatory factors
AU3600199A (en) A pharmaceutical composition containing ezrin mutated on tyrosine 353
GR3001035T3 (en) Heterocyclic tetrahydro-3,4-diamine-n-n'-platinum complexes
EP1003516A4 (en) Methods of administering camptothecin compounds for the treatment of cancer with reduced side effects
CA2283450A1 (en) Methods for treatment of scar tissue
EP0302421A3 (en) Alpha-carotene for inhibiting the growth of cancer cells
YU46302A (en) Substituted pyrroles

Legal Events

Date Code Title Description
EEER Examination request
MKLA Lapsed